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Trifluoroacetic acid → 3-(3-Amino-6-(4-(isopropylsulfonyl)phenyl)pyrazin-2-yl)-1-phenylprop-2-yn-1-one

HRID 78292
ノート
印刷プレビュー

反応式

HRID 78292 の反応式
C(OC([N:8]([C:16]1[C:21]([C:22]#[CH:23])=[N:20][C:19]([C:24]2[CH:29]=[CH:28][C:27]([S:30]([CH:33]([CH3:35])[CH3:34])(=[O:32])=[O:31])=[CH:26][CH:25]=2)=[CH:18][N:17]=1)C(=O)OC(C)(C)C)=O)(C)(C)C.[C:36](Cl)(=[O:43])[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(O)(C(F)(F)F)=O>C1COCC1.C(Cl)Cl.Cl[Pd]Cl.[Cu]I>[NH2:8][C:16]1[C:21]([C:22]#[C:23][C:36]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)=[O:43])=[N:20][C:19]([C:24]2[CH:29]=[CH:28][C:27]([S:30]([CH:33]([CH3:34])[CH3:35])(=[O:32])=[O:31])=[CH:26][CH:25]=2)=[CH:18][N:17]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 6422Trifluoroacetic acidHCID 7412Benzoyl chlorideHCID 11776TriphenylphosphineHCID 59471983N,N-Di(Boc)-3-ethynyl-5-[4-(isopropylsulfonyl)phenyl]pyrazin-2-amine

生成物 1

HCID 866827683-(3-Amino-6-(4-(isopropylsulfonyl)phenyl)pyrazin-2-yl)-1-phenylprop-2-yn-1-one

試薬・触媒・溶媒 4

HCID 24290
Palladium Chloride
触媒
HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒
HCID 6344Dichloromethane溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

tert-butyl N-tert-butoxycarbonyl-N-[3-ethynyl-5-(4-isopropylsulfonylphenyl)pyrazin-2-yl]carbamate (200 mg, 0.3987 mmol), benzoyl chloride (56.04 mg, 46.28 μL, 0.3987 mmol), TEA (44.38 mg, 61.13 μL, 0.4386 mmol) was added to a solution of dichloropalladium; triphenylphosphane (27.98 mg, 0.03987 mmol) and CuI (15.19 mg, 0.07974 mmol) in degassed THF (4 mL). The reaction mixture was stirred overnight at ambient temperature. The reaction mixture was concentrated in vacuo. The residue was partitioned between DCM and NaHCO3 aq sat. The combined organic extract was dried (MgSO4) and concentrated in vacuo yielding an oil that was dissolved in DCM (10 mL). TFA (1 mL) was added and the mixture was stirred at ambient temperature for 30 min. The mixture was concentrated in vacuo to provide the sub-titled product which was used in the next reaction without further purification. LC/MS m/z 406.1 [M+H]+.

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customThe residue was partitioned between DCM and NaHCO3 aq sat. The combined
  3. extractionorganic extract
  4. dry with materialwas dried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customyielding an oil that
  7. stirringthe mixture was stirred at ambient temperature for 30 min
  8. concentrationThe mixture was concentrated in vacuo

出典と根拠

ORDレコード
ord-4454b3409bb046f98aee3cc823e0b096
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08841337B2

反応ノート

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